About Paul Quinn

Paul is a qualified person with over 18 years of experience in the pharmaceutical industry. Paul graduated from Dublin City University with a degree in Chemical and Pharmaceutical Science in 2001. He has held a number of laboratory-based roles with Athlone Laboratories, Pfizer and Allergan before moving into quality assurance in 2009.

First IMP Batch

2022-09-27T14:18:12+01:00September 20th, 2022|

We’re pleased to announce that our team at JensonR+ have released our first Investigational Medicinal Products (IMP) batch. Our quality team have made the final sign-off marking the culmination of the quality process through which a batch of IMP has been shown to conform to all aspects of Good Manufacturing Practice (GMP).

Are you getting value from your PQR process?

2022-01-26T14:26:17+00:00April 28th, 2020|

Pharmaceutical companies and in particular small to medium sized ones, are in a perpetual battle to increase efficiency and reduce costs while staying GMP compliant. The always moving landscape of regulatory compliance puts significant demands on the sometimes-limited resources available to these companies. This can result in the prioritisation of activities of seemingly more importance which will inevitably, despite best efforts, lead to the neglect of others.

Go to Top